(Levonorgestrel + meloxicam) is under clinical development by Innovagyn and currently in Phase II for Female Contraception. According to GlobalData, Phase II drugs for Female Contraception have an 84% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how (Levonorgestrel + meloxicam)’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

(Levonorgestrel + meloxicam) overview

A fixed dose combination of levonorgestrel and meloxicam is under development for female contraception. The therapeutic candidate is administered through oral route. Levonorgestrel acts by targeting progesterone receptor and and meloxicam acts by targeting cyclooxygenase enzymes COX-1 and COX-2.

Innovagyn overview

Innovagyn focuses on novel female oral contraceptive. Innovagyn is headquartered in Portsmouth, New Hampshire, the US.

For a complete picture of (Levonorgestrel + meloxicam)’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

Data Insights


The gold standard of business intelligence.

Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.


GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.